US564835A - Sigmund neumann - Google Patents
Sigmund neumann Download PDFInfo
- Publication number
- US564835A US564835A US564835DA US564835A US 564835 A US564835 A US 564835A US 564835D A US564835D A US 564835DA US 564835 A US564835 A US 564835A
- Authority
- US
- United States
- Prior art keywords
- soap
- fluorescent
- sigmund
- neumann
- fluid
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000000344 soap Substances 0.000 description 24
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 11
- 239000012530 fluid Substances 0.000 description 8
- 238000004519 manufacturing process Methods 0.000 description 7
- 239000012670 alkaline solution Substances 0.000 description 4
- 229910021529 ammonia Inorganic materials 0.000 description 4
- 230000007935 neutral effect Effects 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- GNBHRKFJIUUOQI-UHFFFAOYSA-N fluorescein Chemical class O1C(=O)C2=CC=CC=C2C21C1=CC=C(O)C=C1OC1=CC(O)=CC=C21 GNBHRKFJIUUOQI-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- ACNUVXZPCIABEX-UHFFFAOYSA-N 3',6'-diaminospiro[2-benzofuran-3,9'-xanthene]-1-one Chemical compound O1C(=O)C2=CC=CC=C2C21C1=CC=C(N)C=C1OC1=CC(N)=CC=C21 ACNUVXZPCIABEX-UHFFFAOYSA-N 0.000 description 1
- PLXMOAALOJOTIY-FPTXNFDTSA-N Aesculin Natural products OC[C@@H]1[C@@H](O)[C@H](O)[C@@H](O)[C@H](O)[C@H]1Oc2cc3C=CC(=O)Oc3cc2O PLXMOAALOJOTIY-FPTXNFDTSA-N 0.000 description 1
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 1
- WNBCMONIPIJTSB-BGNCJLHMSA-N Cichoriin Natural products O([C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1)c1c(O)cc2c(OC(=O)C=C2)c1 WNBCMONIPIJTSB-BGNCJLHMSA-N 0.000 description 1
- PLXBWHJQWKZRKG-UHFFFAOYSA-N Resazurin Chemical compound C1=CC(=O)C=C2OC3=CC(O)=CC=C3[N+]([O-])=C21 PLXBWHJQWKZRKG-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- JBBPTUVOZCXCSU-UHFFFAOYSA-L dipotassium;2',4',5',7'-tetrabromo-4,7-dichloro-3-oxospiro[2-benzofuran-1,9'-xanthene]-3',6'-diolate Chemical compound [K+].[K+].O1C(=O)C(C(=CC=C2Cl)Cl)=C2C21C1=CC(Br)=C([O-])C(Br)=C1OC1=C(Br)C([O-])=C(Br)C=C21 JBBPTUVOZCXCSU-UHFFFAOYSA-L 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- YQGOJNYOYNNSMM-UHFFFAOYSA-N eosin Chemical compound [Na+].OC(=O)C1=CC=CC=C1C1=C2C=C(Br)C(=O)C(Br)=C2OC2=C(Br)C(O)=C(Br)C=C21 YQGOJNYOYNNSMM-UHFFFAOYSA-N 0.000 description 1
- IINNWAYUJNWZRM-UHFFFAOYSA-L erythrosin B Chemical compound [Na+].[Na+].[O-]C(=O)C1=CC=CC=C1C1=C2C=C(I)C(=O)C(I)=C2OC2=C(I)C([O-])=C(I)C=C21 IINNWAYUJNWZRM-UHFFFAOYSA-L 0.000 description 1
- XHCADAYNFIFUHF-TVKJYDDYSA-N esculin Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC(C(=C1)O)=CC2=C1OC(=O)C=C2 XHCADAYNFIFUHF-TVKJYDDYSA-N 0.000 description 1
- 229940093496 esculin Drugs 0.000 description 1
- AWRMZKLXZLNBBK-UHFFFAOYSA-N esculin Natural products OC1OC(COc2cc3C=CC(=O)Oc3cc2O)C(O)C(O)C1O AWRMZKLXZLNBBK-UHFFFAOYSA-N 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/0095—Solid transparent soaps or detergents
Definitions
- This invention relates to the production of fluorescent soaps, whether colored or not.
- Ordinary opaque or non-translucent soap is capable of taking up, during its manufacture, fluorescent bodies; but suchjfsoaps do not exhibit in their finished state the characteristics of fluorescence.
- the fluoresent bodies which I may employ by addition to the fluid transparent soap for producing the fluorescence are, for example, fluorescein derivative, eosin, phloxin, erythrosin, saifranin, esculin, rhodamin, azoresorcin, azoresorufin, and their derivatives.
- the fluorescent body is mixed with the fluid soap either in the dry state or in solution by efiective stirring. The soap may then be finished in the usual manner.
- the required coloring-matter may be addedto it after the mixture therewith of the fluorescent body.
- the fluorescent body and of the ammoniacal ingredient are mixed with one kilogram of the fluid soap.
- the quantity may be altered according to the nature of the soap, the fluorescent, and the ammoniacal ingredient. All ammonia compounds which are soluble in water, and which with the addition of caustic alkali produce ammonia, may be employed, especially sal-ammoniac, sulfate of ammonia, and carbonateo fammonia.
- the fluorescent body, the ammoniacal ingredient, and the coloring-matter can be added to the fluid soap in any desired order.
- a new composition of matter consisting of transparent soap and organic bodies which are fluorescent in a neutral or alkaline solution, substantially as described.
- a fluorescent soap consisting of transparent soap, ammonia compounds, and organic bodies which are fluorescent in a neutral or alkaline solution, substantially as described.
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Investigating Or Analysing Biological Materials (AREA)
Description
' which in itself or in its solution is fluorescent UNITED STATES PATENT OFFICE.
SIGMUND NEUMANN, OF BUDA-PESTH, AUSTRIA-HUNGARY.
FLUORESCENT SOAP.
SPECIFICATION 'formingpart of Letters Patent No. 564,835, dated J uly 28, 1896.
Application filed September 14, 1894. Serial No. 523,030. (No specimens.) Patented in Hungary August 16, 1894, No. 1,401; in Austria August 22,1894,No.45/2,348; in Belgium August 22,1894,No. 111,511; in England August 23, 1894, No.
16,040, and in France September 4,1894,N0. 241,112.
To all whom it may concern:
Be it known that I, SIGMUND NEUMANN, of Gottergasse, Buda-Pesth, in the Kingdom of Hungary and Austro-Hungarian Empire, have invented new and useful Improvements in or Connected with the Manufacture of Fluorescent Soaps, (for whichl have obtained the following foreign patents: Austria, No. 45 2,348, dated August 22, 1894; England, No. 16,040, dated August 23, 1894; France, No. 241,112, dated September 4, 1894; Belgium, No. 111,511, dated August 22, 1894, and Hungary, No. 1,401, dated August 16, 1894,) of which the following is a specification.
This invention relates to the production of fluorescent soaps, whether colored or not.
Ordinary opaque or non-translucent soap is capable of taking up, during its manufacture, fluorescent bodies; but suchjfsoaps do not exhibit in their finished state the characteristics of fluorescence.
Instead of employing ordinary non-transparent or non-translucent soap for the purpose of my invention, I take transparent soap during the fluid state of its manufacture, and in this state I add thereto any suitable body and which does not lose its fluorescence inthe finished soap. I may also add to the fluid soap such colors soluble therein as may be desired to produce a given tint or shade. If a solid transparent soapis to be used, the soap may be liquefied by cutting the soap to small pieces and dissolving therfi in alcohol at a temperature of from to centigrade. If the alcohol contains a large quantity of water, the excess of water'in the solution of soap may be evaporated.
The fluoresent bodies which I may employ by addition to the fluid transparent soap for producing the fluorescence are, for example, fluorescein derivative, eosin, phloxin, erythrosin, saifranin, esculin, rhodamin, azoresorcin, azoresorufin, and their derivatives. The fluorescent body is mixed with the fluid soap either in the dry state or in solution by efiective stirring. The soap may then be finished in the usual manner.
If it be desired to impart to the soap a different color to that which may be given to it by the fluorescent body, the required coloring-matter may be addedto it after the mixture therewith of the fluorescent body.
I have found that when using fluorescein or its derivatives for the purpose of this invention the fluorescent effect may be increased by the addition of ammonia or ammonia compounds, and I may accordingly employ these substances in such cases.
As a rule, from one to two milligrams of the fluorescent body and of the ammoniacal ingredient are mixed with one kilogram of the fluid soap. The quantity, however, may be altered according to the nature of the soap, the fluorescent, and the ammoniacal ingredient. All ammonia compounds which are soluble in water, and which with the addition of caustic alkali produce ammonia, may be employed, especially sal-ammoniac, sulfate of ammonia, and carbonateo fammonia. The fluorescent body, the ammoniacal ingredient, and the coloring-matter can be added to the fluid soap in any desired order.
What I claim, and desire to secure by Letters Patent of the United States, is-
1. A new composition of matter consisting of transparent soap and organic bodies which are fluorescent in a neutral or alkaline solution, substantially as described.
2. As a new article of manufacture, a fluorescent soap, consisting of transparent soap, ammonia compounds, and organic bodies which are fluorescent in a neutral or alkaline solution, substantially as described.
3. The method of making fluorescent soap, consisting in adding to fluid transparent soap organic bodies which are fluorescent in a neutral or alkaline solution, substantially as described.
4. The method of making fluorescent soap, consisting in adding to fluid transparent soap organic bodies which are fluorescent in a neutral or alkaline solution, and also ammonia or its compounds; substantially as described.
In witness whereof I have hereunto set my hand in presence of two witnesses.
SIGMUND NEUMANN.
Witnesses:
HANS BAUERLEIN, MAXIMILIAN Minx.
Publications (1)
Publication Number | Publication Date |
---|---|
US564835A true US564835A (en) | 1896-07-28 |
Family
ID=2633552
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US564835D Expired - Lifetime US564835A (en) | Sigmund neumann |
Country Status (1)
Country | Link |
---|---|
US (1) | US564835A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2590485A (en) * | 1939-06-02 | 1952-03-25 | Lever Brothers Ltd | Process of treating yellowish or off-white materials to obtain a white appearance using umbelliferone or methyl umbelliferone |
US2763650A (en) * | 1956-09-18 | Derivatives of x | ||
US2778827A (en) * | 1949-10-28 | 1957-01-22 | Ciba Ltd | Process for the manufacture of derivatives of 4:4'-diaminostilbene-2:2'-disulfonic acid |
US2805999A (en) * | 1949-10-18 | 1957-09-10 | Ciba Ltd | Detergent compositions containing derivatives of 4:4'-diaminostilbene-disulfonic acid |
US2846397A (en) * | 1949-10-14 | 1958-08-05 | Ciba Ltd | Water-soluble salts of derivatives of 4:4'-diaminostilbene-2:2'-disulfonic acid for enhancing the brightness of organic fibrous material |
-
0
- US US564835D patent/US564835A/en not_active Expired - Lifetime
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2763650A (en) * | 1956-09-18 | Derivatives of x | ||
US2590485A (en) * | 1939-06-02 | 1952-03-25 | Lever Brothers Ltd | Process of treating yellowish or off-white materials to obtain a white appearance using umbelliferone or methyl umbelliferone |
US2846397A (en) * | 1949-10-14 | 1958-08-05 | Ciba Ltd | Water-soluble salts of derivatives of 4:4'-diaminostilbene-2:2'-disulfonic acid for enhancing the brightness of organic fibrous material |
US2805999A (en) * | 1949-10-18 | 1957-09-10 | Ciba Ltd | Detergent compositions containing derivatives of 4:4'-diaminostilbene-disulfonic acid |
US2778827A (en) * | 1949-10-28 | 1957-01-22 | Ciba Ltd | Process for the manufacture of derivatives of 4:4'-diaminostilbene-2:2'-disulfonic acid |
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